不同厂家的三种普洱红茶的FTIR研究

采用博里叶变换红外光谱法(FTIR)获取了不同厂家不同年份的三种普洱红茶的红外光谱, 并对所得的指纹图谱进行特征峰指认和对比分析.结果表明:这三种茶叶的化学成分基本相同,而由于各成分间的相对含量不同,使每种茶叶都有自己独特的红外谱图,另外,对于存储年份相对较长的茶叶的谱图,第一吸收峰峰位偏向低波数方向,1306cm-1附近的二肩峰及1369cm-1附近的双峰的峰强比存储年份较短的茶叶的峰强更弱,峰形更宽.这一结果说明,FTIR对于鉴别"普洱茶"的真伪及存储年份有一定的参考价值.     

全光纤干涉式结构中传感模式仿真分析

全光纤干涉式传感结构中包层模场与外界物理量作用,携带被感测信息,因此对包层模的研究是设计制作和提高该类传感器传感性能的关键.利用有限差分光束传播法获得传感光纤不同长度和不同芯径比时传感器对应的光谱,通过傅里叶变换获得其干涉频谱,计算出各主要参与干涉的包层模组的有效折射率,利用色散方程确定对应包层模.理论仿真结果显示,随着传感部分光纤长度增加,参与干涉的包层模式随之增加,并且向高阶模式变化,光谱变得稠密,是多阶包层模干涉的叠加,传感器输出干涉谱的自由光谱范围变小.随着输入光纤与传感光纤芯径比变化,会明显改变纤芯包层功率分布,同时,芯径比增大也会增加参与干涉的包层模种类和阶数.     

Cu2+掺杂CdS纳米晶的制备与表征

以巯基乙酸为稳定剂,采用水相合成法制备了Cu2+掺杂的CdS纳米晶. 分别用电感耦合等离子体发射光谱仪、原子力显微镜测试技术对样品的化学成分及形状进行分析表征,研究了掺杂CdS纳米晶的荧光激发与发射光谱. 实验结果表明,在样品制备过程的溶液中回流2 h后,组成为Cd0.99Cu0.01S的样品形状有棒状和粒状2种,Cu2+的掺入使得CdS纳米晶的荧光发射光谱红移,没有掺杂的样品在回流前的最大发射波长在520 nm处,而组成为Cd0.99Cu0.01S和Cd0.98Cu0.02S的样品在回流前的最大发射波长分别为595和610 nm,通过改变Cu与Cd摩尔比可调控CdS纳米晶的发射波长范围.     

Ⅱ型TiO2/g-C3N4异质结的构筑促进高效光催化U(Ⅵ)还原

采用水热法将TiO₂纳米片修饰在中空管状g-C₃N₄上制备了TiO₂/g-C₃N₄(T-CN)复合催化剂。利用扫描电子显微镜(SEM)、X射线光电子能谱(XPS)、紫外可见漫反射光谱(UV-Vis DRS)和光电流响应等对其形貌、结构和光物理性能进行了表征。结果表明,TiO₂纳米片均匀地分散在中空管状g-C₃N₄表面,两者紧密结合形成异质结。TiO₂与g-C₃N₄的质量比为20%时制得的T-CN-20复合催化剂在60 min内对U的去除率为85.64%,是纯相g-C₃N₄的6.7倍。在10倍高浓度阳离子共存条件下的去除率仍大于69.8%,且具有优良的结构稳定性。对光催化产物分析可知,T-CN将U还原为难溶的U(63.68%)以去除铀,可有效解决含铀核废水中的U污染问题。根据能带理论分...     

气液色谱有限浓度法研究醇类在芳烃溶剂中的自缔合及交叉缔合

气液色谱有限浓度法研究醇类在芳烃溶剂中的自缔合及交叉缔合王毅琳,周效贤,李松林,郑国康（兰州大学化学系,兰州,７３００００）关键词醇,自缔合,交叉缔合前文［１］用气液色谱有限浓度法研究了Ｃ４各正构醇在角鲨烷中的活度系数．本文报道在３１３．１５Ｋ下对Ｃ...     

Spatial distribution of electron characteristic in argon rf glow discharges

The spatial distributions of the electron density and the mean electron energy of argon radio frequency (rf) glow discharge plasma in a plasma-enhanced chemical vapour deposition (PECVD) system have been investigated using an established movable Langmuir probe. The results indicate that in the axial direction the electron density tends to peak at midway between the two electrodes while the axial variation trend of mean electron energy is different from that of the electron density, the mean electron energy is high near the electrodes. And the mean electron energy near the cathode is much higher than that near the anode. This article focuses on the radial distribution of electron density and mean electron energy. A proposed theoretical model distribution agrees well with the experimental one: the electron density and the mean electron energy both increase from the centre of the glow to the edge of electrodes. This is useful for better understanding the discharge mechanism and searching for a better deposition condition to improve thin film quality.     

Tetrazole Diversification of Amino Acids and Peptides via Silver-Catalyzed Intermolecular Cycloaddition with Aryldiazonium Salts

Selective structural modification of amino acids and peptides is a central strategy in organic chemistry, chemical biology but also in pharmacology and material science. In this context, the formation of tetrazole rings, known to possess significant therapeutic properties, would expand the chemical space of unnatural amino acids but has received less attention. In this study, we demonstrated that the classic unimolecular Wolff rearrangement of α-amino acid-derived diazoketones could be replaced by a faster intermolecular cycloaddition reaction with aryldiazonium salts under identical practical conditions. This strategy provides an efficient synthetic platform that could transform proteinogenic α-amino acids into a plethora of unprecedented tetrazole-decorated amino acid derivatives with preservation of the stereocenters. Density functional theory studies shed some light on the reaction mechanism and provided information regarding the origins of the chemo- and regioselectivity. Furthermore, this diazo-cycloaddition protocol was applied to construct tetrazole-modified peptidomimetics and drug-like amino acid derivatives.